ライフサイエンスコーパス: cellulose

1 recalcitrant substrates including chitin and cellulose.

2 sts a conserved specialization for growth on cellulose.

3 nd to be important in binding to crystalline cellulose.

4 e believed to be mostly, if not exclusively, cellulose.

5 including symbiotic polysaccharide (Syp) and cellulose.

6 nfer the remarkable structural properties of cellulose.

7 ect two populations of water associated with cellulose.

8 and the maximum binding capacity of LPMO for cellulose.

9 ulase to function well on highly crystalline cellulose.

10 smaller leaves and a loss of the content of cellulose.

11 ong-time knowledge and easy manufacturing of cellulose.

12 erm xylan binding to hydrophilic surfaces of cellulose.

13 to polyphenol adsorption in the presence of cellulose.

14 (PAS) highlighted the presence of starch and cellulose.

15 tial enzyme hydrolysis of hemicelluloses and cellulose.

16 lecules was predominant for the pyrolysis of cellulose.

17 1 mucilage exhibited very weak adsorption to cellulose.

18 carbon sink and a renewable source of ligno-cellulose.

19 thin the tumor through the addition of ethyl cellulose.

20 atrix consisting of curli amyloid fibers and cellulose.

21 erved as a model system for the breakdown of cellulose.

22 oxygen species increased the affinity toward cellulose.

23 Microcrystalline cellulose (100-500 mg), used as a combustion aid, was mi

24 6 healthy individuals were supplemented with cellulose (30 g/d), inulin (30 g/d), or propionate (6 g/

25 The use of cellulose (400 mg) was mandatory to volatilize the halog

26 the mucoadhesive properties of carboxymethyl cellulose, a commonly used polysaccharide in the food an

27 factor CLR-1 is necessary for utilization of cellulose, a major, recalcitrant component of the plant

28 s the effect of dietary supplementation with cellulose, a nonfermentable fiber, on the gut microbiota

29 first modification was the application of a cellulose acetate (CA) gas permeable membrane.

30 animal adhesion on two different substrates (cellulose acetate and polydimethylsiloxane) in air and f

31 e dependence on sample pH, and an underlying cellulose acetate filter membrane coated with protamine

32 The LIS consists of two cellulose acetate membranes: the conjugate pad capturing

33 We describe cellulose acetate-derived carbons that combine high surf

34 r C1/C4-oxidizing, but not for C1-oxidizing, cellulose-active LPMO10s.

35 ional ELM: the water saturated nanocellulose cellulose aerogel microspheres can be easily removed by

36 loxane network with further incorporation of cellulose, allows for an increase of density as well as

37 Hence, breakdown of cellulose along with pectin and starch is important for

38 ls of both fermentable sugars and hydrolyzed cellulose and altered cell wall properties such as highe

39 to recognize different crystalline forms of cellulose and chitin over a wide range of temperatures,

40 nds in recalcitrant polysaccharides, such as cellulose and chitin, and are of interest in biotechnolo

41 rant polysaccharides found in nature, namely cellulose and chitin.

42 aces but that they increase the affinity for cellulose and favor the stabilization of the 2-fold scre

43 sic feed followed by oxygen removal from its cellulose and hemicellulose content by catalytic process

44 e importance of the cellulosome paradigm for cellulose and hemicellulose degradation by R. champanell

45 nificant changes occurred in the contents of cellulose and hemicellulose that increased 37% and 28%,

46 lls of NPC1-OE plants have lower contents of cellulose and hemicellulose, and thinner sclerenchyma an

47 ccinivibrio, which promotes the digestion of cellulose and hemicellulose, was significantly increased

48 Xylan is tightly associated with cellulose and lignin in secondary plant cell walls, cont

49 onservation, allowing the degradation of the cellulose and lignin polymeric components of the woods t

50 ured by saturated carboxylic acids from hemi/cellulose and lipids with concentrations decreasing with

51 om Neurospora crassa, which is active toward cellulose and soluble beta-glucans, to study the enzyme-

52 using pond sediment and water, enriched with cellulose and sulphate, and allowed to develop over seve

53 stomatal closure, indicating that sufficient cellulose and xyloglucan are required for normal guard c

54 howed a stabilizing effect of the substrates cellulose and xyloglucan on the apparent transition midp

55 alone, AC with slow release electron donor (cellulose) and different concentrations and combinations

56 ct that naturally occurring forms of starch, cellulose, and chitin can have tightly packed organizati

57 atural carbohydrate polymers such as starch, cellulose, and chitin provide renewable alternatives to

58 alyst performs hydrodeoxygenation of lignin, cellulose, and hemicellulose-derived oligomers into liqu

59 bran-related compounds such as arabinoxylan, cellulose, and lipids.

60 Xylan and cellulose are abundant polysaccharides in vascular plant

61 amorphous while the surface layers of Ibeta cellulose are crystalline but with different structural

62 ymethylcellulose and phosphoric acid-swollen cellulose are in fact relatively poor substrates for PbG

63 Interactions of water with cellulose are of both fundamental and technological impo

64 results indicate that oligomers derived from cellulose are perceived as signal molecules in Arabidops

65 osiruptor bescii degrades highly crystalline cellulose as well as low crystallinity substrates making

66 ance in enhancing chemical deconstruction of cellulose, as it permits an increase in potential THF-wa

67 een ordered domains when Cel7A is engaged on cellulose, as models predict alpha-helix formation and d

68 aeticus (K. rhaeticus iGEM) that can produce cellulose at high yields, grow in low-nitrogen condition

69 rulic acid and cyanidin-3-glucoside bound to cellulose-based composites and apple cell walls with dif

70 s exhibited binding selectivity to different cellulose-based composites and apple cell walls.

71 via preparative column chromatography using cellulose-based stationary phases and step-gradient aque

72 exceeding that of even biological silks and cellulose-based viscose rayon.

73 Our results suggest that cellulose beta-1-4 linkages can be cut sparingly in the

74 odule increases the affinity of HjLPMO9A for cellulose binding, but does not affect the active site.

75 onsisting of an rcSso7d binding module and a cellulose-binding domain.

76 c, and circadian clock signaling on rates of cellulose biosynthesis and cell wall biomechanics.

77 stituted PttCesA8 is not only sufficient for cellulose biosynthesis in vitro but also suffices to bun

78 sly shown in other systems to be involved in cellulose biosynthesis, hemicellulose biosynthesis, seco

79 or characterized genes involved in xylan and cellulose biosynthesis, regulators of xylem vessel and f

80 ase complex, and thereby negatively regulate cellulose biosynthesis.

81 d that the cDNA fragment was relevant to the cellulose biosynthesis.

82 emonstrating that enhanced solubilization of cellulose can be achieved by the THF-water co-solvent sy

83 Overall, mean background binding to cellulose CCDs corresponded to 2% to 3% of the reactivit

84 ers oriented such that the newly synthesized cellulose chains project toward the cell membrane.

85 crystalline cellulose (MCC) or carboxymethyl cellulose (CMC) can be used as fat replacers; both are n

86 Nano-ZnO in combination with carboxymethyl cellulose (CMC) coating was used on pomegranate arils.

87 The platforms included (i) cellulose-coated microarray assay, (ii) enzyme-linked im

88 exhibited reduced binding to and activity on cellulose compared with the full-length enzyme.

89 , however, the total amount the median water-cellulose contact lifetimes increases for the cosolvent

90 mount combined with the relative increase in cellulose content in the CSE down-regulated lines result

91 ity in an apical-to-basal pattern, while the cellulose content increased modestly.

92 s for the further study of modulation of the cellulose content of crops.

93 es the reduction in hypocotyl elongation and cellulose content of shv3svl1 This effect was specific t

94 the lignin polymer, and a relatively higher cellulose content.

95 acts from tannin and non-tannin sorghum, and cellulose control, were reacted with normal and waxy mai

96 te that N-glycosylation has little impact on cellulose conversion or binding, but does have major sta

97 However, linker O-glycans greatly impact cellulose conversion via their contribution to proteolys

98 combined with fine milling slightly reduced cellulose crystallinity.

99 ion, electrode material, hydrophobization of cellulose, dedicated electrochemical devices and electro

100 The cellulose-deficient midribs of ppcesa3/8 knockouts provi

101 a low-diversity state that followed initial cellulose degradation and sulphate reduction.

102 sed the catalytic efficiency of a commercial cellulose-degrading enzyme cocktail by 2.4-fold.

103 ial of DeltaxlnR to secrete arabinoxylan and cellulose-degrading enzymes and indicates that XlnR is t

104 sional structures for almost all H. jecorina cellulose-degrading enzymes are available, except for Hj

105 is consistent with the observed increase in cellulose deposition in the internodes of 35S::SbMyb60 p

106 anoparticles, a semicrystalline hydroxyethyl cellulose derivative, and cucurbit[8]uril undergo aqueou

107 Thus, the perception of cellulose-derived oligomers may participate in cell wall

108 end-product formation during fermentation of cellulose-derived sugars.

109 elongation rate in response to inhibitors of cellulose (dichlorobenylnitrile; DCB), microtubules (ory

110 ids and hepatoma cells by gas chromatography.Cellulose did not affect plasma OCFA levels, whereas inu

111 mented a synergistic action of expansins for cellulose digestion by cellulases, but only rarely to an

112 eported for the first time in the context of cellulose discoloration.

113 ce and whether this alters a purely physical cellulose dissociation pathway.

114 In contrast, ethyl cellulose-ethanol injections of one-fourth the tumor vol

115 he interpretation that water associated with cellulose exists in two dynamical populations.

116 The hydrogels prepared from the cellulose extracted from rice and oat husks showed water

117 fiber sources tested, psyllium, pectin, and cellulose fiber reduced the severity of colitis in SPF m

118 ile fermentable (inulin), but not insoluble (cellulose), fiber markedly protected mice against high-f

119 The commercial cellulose fibers and cellulose fibers extracted from ric

120 The commercial cellulose fibers and cellulose fibers extracted from rice and oat husks were

121 The cellulose fibers from rice and oat husks were used to pr

122 The hydrogel from rice cellulose fibers had a network structure with a similar

123 eous pores compared to the hydrogel from oat cellulose fibers.

124 tiple xylan chains to adjacent planes of the cellulose fibril stabilizes the interaction further.

125 ing behaviour controlled by the alignment of cellulose fibrils along prescribed four-dimensional prin

126 teraction of xylan with hydrophilic faces of cellulose fibrils, and is essential for development of n

127 stantially cut the "natural" chain length of cellulose fibrils.

128 tions, xylan does not interact normally with cellulose fibrils.

129 1:9 incorporated with blended carboxymethyl cellulose film increased the water barrier and the TPC.

130 ally designed bottlebrush-like hydroxypropyl cellulose-graft-poly (acrylic acid) (HPC-g-PAA) as a tem

131 naturally a composite material, comprised of cellulose, hemicellulose, and lignin.

132 thogens, is composed of a complex mixture of cellulose, hemicellulose, and pectin polysaccharides as

133 al syntheses of oligosaccharide fragments of cellulose, hemicellulose, pectin, and arabinogalactans,

134 nd biomarkers derived from thermally altered cellulose/hemicellulose (anhydrosugars) and lignin (meth

135 omass for biofuel production, is composed of cellulose, hemicelluloses, pectins and lignin.

136 tress the compression were presented by rice cellulose hydrogel at 25 degrees C.

137 have supramolecular structures for enzymatic cellulose hydrolysis that are distinct from cellulosomes

138 s cellulose nanocrystals and nanofibers with cellulose I and II structures (cellulose nanocrystals (C

139 loses and transform cellulose structure from cellulose I to cellulose II, was competent to prepare SR

140 form cellulose structure from cellulose I to cellulose II, was competent to prepare SREL as an ideal

141 In this work, regenerated cellulose immuno-affinity membranes were developed and t

142 partitioning of carbon to starch rather than cellulose in both mutants.

143 -fold screw xylan binds hydrophilic faces of cellulose in eudicots, early-branching angiosperm, and g

144 ike twofold screw conformation when bound to cellulose in the cell wall (4) .

145 ght networks of polysaccharides intertwining cellulose in the plant cell wall, thus increasing access

146 e surfaces and partially deconstruct Avicel (cellulose) in the absence of acid.

147 arbon isotope discrimination (Delta(13)C) in cellulose indicates the favorability of conditions for p

148 anges are connected with increases in pectin-cellulose interaction and reductions in wall compliances

149 predict alpha-helix formation and decreased cellulose interaction for the nonglycosylated linker.

150 ilizes an enigmatic mechanism to deconstruct cellulose into cellobiose and glucose, which serve as ca

151 tary fibre polysaccharides (microcrystalline cellulose, inulin, apple pectin and citrus pectin) durin

152 The deposition of cellulose is a defining aspect of plant growth and devel

153 Cellulose is a linear glucose polymer synthesized and se

154 Cellulose is a major component of the cell wall and cell

155 By contrast, the biosynthesis of cellulose is controlled through intracellular traffickin

156 Deconstruction of cellulose is crucial for the chemical conversion of lign

157 actions, even while the amount of water near cellulose is decreased.

158 iotic niches, the ability to rapidly degrade cellulose is largely restricted to two clades of host-as

159 In plants, cellulose is produced by cellulose synthase, a processiv

160 enone (LGO) is the major product formed when cellulose is pyrolyzed in the presence of acid at temper

161 An in vitro system in which cellulose is synthesized and assembled into fibrils woul

162 For catechin, cellulose is the dominant binding component, whereas hem

163 Cellulose is the major component of cell wall materials.

164 urely physical process for deconstruction of cellulose is unlikely for these cosolvents, and in THF-w

165 t ingredients (guar, xanthan, carboxy methyl cellulose, locust bean gums, potato fiber, milk, potato

166 The resulting bacterial cellulose macrofibers yield record high tensile strength

167 hydration and diffusion of the hydroxypropyl cellulose matrix is presented.

168 e homogeneous permeation of fluids along the cellulose matrix than other existing designs in the lite

169 g of heterologous gene expression within the cellulose matrix.

170 Microcrystalline cellulose (MCC) or carboxymethyl cellulose (CMC) can be

171 iple windows containing a porous regenerated-cellulose membrane with a molecular-weight cutoff of app

172 trophotometric methods, protein diffusion on cellulose membranes and electrophoretic protein profiles

173 l (CC) using laccase immobilized on graphene-cellulose microfibers (GR-CMF) composite modified screen

174 king of xylan onto the hydrophilic face of a cellulose microfibril (1-3) .

175 collected from midribs were consistent with cellulose microfibril aggregation, and polarization micr

176 ll structure, including a slight increase in cellulose microfibril alignment along the growing stem.

177 nthesis complex that synthesizes an 18-chain cellulose microfibril as its fundamental product.

178 abeled Glc, linkage analysis, and imaging of cellulose microfibril formation using transmission elect

179 has been hypothesized to bind extensively to cellulose microfibril surfaces and to tether microfibril

180 ellulose, are often considered as spacers of cellulose microfibrils during growth.

181 an appreciable, but still small, surface of cellulose microfibrils in the onion wall is tightly boun

182 tructural reinforcement of the wall by stiff cellulose microfibrils is central to contemporary models

183 The crystalline nature of cellulose microfibrils is one of the key factors influen

184 e, each ~40 nm thick, containing 3.5-nm wide cellulose microfibrils oriented in a common direction wi

185 of tracheary elements and fibers are rich in cellulose microfibrils that are helically oriented and l

186 e forces that control the interactions among cellulose microfibrils, hemicelluloses, and lignin are s

187 opy depend on the orientation of crystalline cellulose microfibrils, their bonding to the polysacchar

188 e pectin-rich cell wall matrix embedded with cellulose microfibrils, we show that strong, circumferen

189 ices to bundle individual glucan chains into cellulose microfibrils.

190 ntrast to the application of cream and ethyl cellulose nanocarriers, Dex was already detectable in el

191 Pure cellulose nanocrystal (CNC) aerogels with controlled 3D

192 The fabrication of self-assembled cellulose nanocrystal (CNC) films of tunable photonic an

193 Herein, we show that rod-like cellulose nanocrystal (CNC)-based NP-surfactants, termed

194 eviously coated with thin films of bacterial cellulose nanocrystals (CN) to provide a more sensitive

195 nofibers with cellulose I and II structures (cellulose nanocrystals (CNC) I, CNC II, cellulose nanofi

196 avior of four nanocellulose samples, such as cellulose nanocrystals and nanofibers with cellulose I a

197 large variety of biological building blocks, cellulose nanocrystals are one of the most promising bio

198 from colloidal liquid crystal suspensions of cellulose nanocrystals are reviewed and recent advances

199 The self-assembly of cellulose nanocrystals is a powerful method for the fabr

200 Cellulose nanofiber (CNF)-based emulsion coating (CNFC:

201 e of graphene nanosheets (GNs) and bacterial cellulose nanofibers (BCNs).

202 res (cellulose nanocrystals (CNC) I, CNC II, cellulose nanofibers (CNF) I, and CNF II) were studied b

203 Cellulose nanofibers are promising building blocks for f

204 Transparent films made of cellulose nanofibers are reported recently.

205 The anisotropic film with well-aligned cellulose nanofibers has a mechanical tensile strength o

206 The well-aligned cellulose nanofibers in natural wood are maintained duri

207 lm mechanical properties on the alignment of cellulose nanofibers through the film thickness directio

208 of that of a film with randomly distributed cellulose nanofibers.

209 wet-twisting process of ultralong bacterial cellulose nanofibers.

210 conductive oxide (TCO) layer on transparent cellulose nanofibril (CNF) papers.

211 The ultra-light cellulose nanofibril based aerogel microspheres with hig

212 Foldable organic memory on cellulose nanofibril paper with bendable and rollable ch

213 Hereby we report a novel cellulose nanofirbril aerogel-based W/O/W microreactor s

214 Cellulose nanomaterials (CNs)-incorporated emulsion coat

215 to implant timolol maleate (TM) loaded ethyl cellulose nanoparticle-laden ring in hydrogel contact le

216 Dietary supplementation with cellulose offers a microbe-mediated survival advantage i

217 Cellulose paper is an ideal diagnostic platform for low-

218 ionophore can also be fabricated directly on cellulose paper strips.

219 Here, we introduce metallic cellulose paper-based supercapacitor electrodes with exc

220 dinonylnaphthalenesulfonate adsorbed to the cellulose paper.

221 ements, the new optode relies on hydrophilic cellulose paper.

222 ed with nanocrystalline and microcrystalline cellulose particles (NCC and MCC, respectively) were pre

223 rganism readily ferments sugars derived from cellulose, pentose sugars from xylan are not metabolized

224 nostearate carbonate-co-caprolactone), and a cellulose/polyester core.

225 previously undescribed genes associated with cellulose production.

226 ins that can interact with CesAs and control cellulose quantity.

227 t permits an increase in potential THF-water-cellulose reactions, even while the amount of water near

228 Although type A CBMs play a critical role in cellulose recycling, their mechanism of action remains p

229 apertures, changes in guard cell length, and cellulose reorganization were aberrant during fusicoccin

230 rmed a screen for unidentified actors in the cellulose-response pathway and identified a gene encodin

231 f surface layers and the crystalline core of cellulose, revealing their differences for the first tim

232 ls within the leaf midribs of mosses deposit cellulose-rich secondary cell walls, but their biosynthe

233 otein-rich walls of chlorophyte algae to the cellulose-rich walls of embryophytes.

234 Significant questions remain in respect to cellulose's structure and polymorphs, particularly the c

235 Porous cellulose sheets also allow the sensing site to be modif

236 anthan, locust bean, guar and carboxy methyl cellulose significantly enhanced Bostwick consistency an

237 ty, and thermal properties, depending on the cellulose source.

238 nting an inert cake model (starch, water and cellulose), specifically designed for mimicking a sponge

239 o fabricate superhydrophobic TiO2 NPs coated cellulose sponge.

240 onsisting of immobilized rennin on a tubular cellulose/starch gel (TC/SG) composite, which has been p

241 ectively remove hemicelluloses and transform cellulose structure from cellulose I to cellulose II, wa

242 ddition, an ultrathin (800-nm) biodegradable cellulose substrate with high chemical and thermal stabi

243 erences between hydrogen bonding networks of cellulose surface and crystalline core were also shown b

244 a-valerolactone) exhibit phase separation at cellulose surface and whether this alters a purely physi

245 s structure and polymorphs, particularly the cellulose surface layers and the bulk crystalline core a

246 Tethering of the released fluorophore to the cellulose surface prevents signal degradation due to dif

247 er) has been shown to both phase-separate on cellulose surfaces and partially deconstruct Avicel (cel

248 lan are not only sterically tolerated by the cellulose surfaces but that they increase the affinity f

249 lan conformation and on the interaction with cellulose surfaces in Norway spruce (Picea abies).

250 degrees of phase-separation of organosolv on cellulose surfaces, physical dissociation is not enhance

251 Although the Cellulose Synthase (CESA) gene families of mosses and se

252 BR) signaling, can phosphorylate Arabidopsis cellulose synthase A1 (CESA1), a subunit of the primary

253 site abolished BIN2-dependent regulation of cellulose synthase activity.

254 The cellulose synthase complex (CSC) exhibits a 6-fold symme

255 (CESA1), a subunit of the primary cell wall cellulose synthase complex, and thereby negatively regul

256 C17 administration depletes cellulose synthase complexes (CSCs) from the plasma memb

257 en studied by characterizing the motility of cellulose synthase complexes tagged with a fluorescent p

258 trolled through intracellular trafficking of cellulose synthase enzyme complexes regulated exclusivel

259 lineage and identify CSLD5, a member of the Cellulose Synthase Like-D family, as a cell wall biosynt

260 Here we characterize cellulose synthase motility in the model grass, Brachypo

261 that in addition to the previously described cellulose synthase operon, ATCC 53582 contains two addit

262 e operon, ATCC 53582 contains two additional cellulose synthase operons and several previously undesc

263 In plants, cellulose is produced by cellulose synthase, a processive family-2 glycosyltransf

264 lographic structure of a rice (Oryza sativa) cellulose synthase, OsCesA8, plant-conserved region (P-C

265 total protein levels, and the expression of CELLULOSE SYNTHASE-LIKE genes.

266 esized and secreted by a membrane-integrated cellulose synthase.

267 Cellulose synthases are required for the biosynthesis of

268 sis thaliana hypocotyl growth, we found that cellulose synthesis and cell expansion can be uncoupled

269 In cesa3(je5) mutants defective in cellulose synthesis and xxt1 xxt2 mutants lacking the he

270 e "hexamer of trimers" model for the rosette cellulose synthesis complex that synthesizes an 18-chain

271 ils is coupled to rapid and highly localized cellulose synthesis enabled by regulatory uncoupling fro

272 The mechanism of cellulose synthesis has been studied by characterizing t

273 mechanism for how BR signaling can modulate cellulose synthesis in plants.

274 se is a major component of the cell wall and cellulose synthesis is pivotal to plant cell growth, and

275 Moreover, modulation cellulose synthesis probably was an important influencin

276 Genes linked to UDP-sugar biosynthesis and cellulose synthesis were also induced, which is consiste

277 oxygen isotopic time series from Taiwan tree cellulose that span from 1190 AD to 2007 AD.

278 Cellulose, the major component of plant cell walls, can

279 nthases are required for the biosynthesis of cellulose, the most abundant biopolymer of plant cell wa

280 Deconstruction of cellulose, the most abundant plant cell wall polysacchar

281 on a polar liquid zwitterion that dissolves cellulose, the most recalcitrant component of the plant

282 cifically bind to the crystalline regions of cellulose, thus promoting enzyme efficacy through proxim

283 Cellulose used as a solid-phase allergen carrier can con

284 We investigated whether cellulose used as an allergen carrier in ImmunoCAP harbo

285 rize the properties of water associated with cellulose using deuterium labeling, neutron scattering a

286 3) glucan utilization, while Bgl3B underpins cellulose utilization and supports MLG utilization.

287 ontain three major types of polysaccharides: cellulose, various hemicelluloses, and pectins.

288 ctural snapshots show that BcsA translocates cellulose via a ratcheting mechanism involving a 'finger

289 expected affinity for bacterial crystalline cellulose was not detected.

290 binds the hydrophobic surface of crystalline cellulose, was infrequent until the wall was predigested

291 mechanism of the THF-water interactions with cellulose, we pair simulation and experimental data demo

292 nd degradation of lignin, hemicelluloses and cellulose were also differentially expressed between sof

293 No apparent changes in cellulose were detected by NMR and synchrotron X-ray dif

294 dentified a suitable binder additive, methyl cellulose, which offers suitable viscosity for printabil

295 e loading by pyrolysis of polyaniline coated cellulose wiper.

296 acetylene black, and 3 wt % of carboxymethyl cellulose with an areal loading higher than 3 mg cm(-2)

297 of the rcSso7d binding species to unmodified cellulose within a 30-second incubation period.

298 tic polysaccharide mono-oxygenases targeting cellulose, xylan, and chitin, were identified.

299 cleave a range of polysaccharides, including cellulose, xyloglucan, mixed-linkage glucan and glucoman

300 rcSso7d-CBD was found to adsorb per gram of cellulose, yielding a volume-averaged binder concentrati